Lithium Hydroxide → HCID 67847834, compound

HRID 1086867Notes

Reaction equation

HRID 1086867 reaction equation
C([O:8][C:9](=[O:39])[C@H:10]([CH2:30][C:31]1[CH:36]=[CH:35][C:34]([O:37][CH3:38])=[CH:33][CH:32]=1)[N:11]([C:20]([O:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:21])[C:12](=[O:19])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH2:18])C1C=CC=CC=1.[Li+].[OH-]>O1CCCC1.O>[C:20]([N:11]([C:12](=[O:19])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH2:18])[C@H:10]([C:9]([OH:39])=[O:8])[CH2:30][C:31]1[CH:36]=[CH:35][C:34]([O:37][CH3:38])=[CH:33][CH:32]=1)([O:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:21]

Participants

5

Procedure

A solution of 2.66 g (5 mmol) of the resultant compound of Example 170 in 60 mL of tetrahydrofuran was cooled to 0° C, treated with 0.63 g (15 mmol) of LiOH in 30 mL of H2O and allowed to stir for 2 h. After concentration of the solvent, the mixture was partitioned between H2O and ether, acidified, extracted with ethyl acetate, dried over MgSO4 and concentrated to give 1.55 g (70%) of the desired compound.

Workup

  1. customAfter concentration of the solvent, the mixture was partitioned between H2O and ether
  2. extractionextracted with ethyl acetate
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-cd7af7018322405795db85c948bf8303
Source dataset
uspto-grants-1991_07
Patent number
US05032577

Reaction notes

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